Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies

Table 1 Mendelian consistencies among HapMap family samples genotyped

Ancestry	FID	HapMap father	HapMap mother	HapMap child	SNP errors observed	P-P-C heritability* (%)
CEU	1334	NA12144	NA12145	NA10846	3,757	99.51
CEU	1340	NA06994	NA07000	NA07029	3,600	99.53
CEU	1340	NA07022	NA07056	NA07019	264	99.97
CEU	1463	NA12891	NA12892	NA12878	869	99.89
YRI	Y004	NA18501	NA18502	NA18500	4,397	99.43
YRI	Y009	NA18507	NA18508	NA18506	4,672	99.39
YRI	Y045	NA19200	NA19201	NA19202	602	99.92
YRI	Y058	NA19223	NA19222	NA19221	936	99.88

*Heritability calculated as (# correct /767203 total SNPs post-QC)
CEU, International HapMap CEPH European descent populations; FID, HapMap family ID; P-P-C, parent-parent-child; YRI, Hapmap Yoruba African samples

ISSN: 1756-994X